HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196673Generated: November 1, 2026
Potassium Carbonate → HCID 67156075, compound
https://huagongshe.com/reaction/2196673
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Methyl-1H-indole-5-boronic acid | HCID 2759867 | — |
| Reactant | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Reactant | HCID 67155817 | HCID 67155817 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water ethylacetate | HCID 22728543 | — |
| Product | HCID 67156075 | HCID 67156075 | 70% |
Reaction Steps
A mixture of 2,6-difluoro-N-(2-iodo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)-3-(propylsulfonamido)benzamide (27 mg, 40 mmol, 1.0 eq.), 1-methyl-1H-indol-5-ylboronic acid (1.5 eq.), K2CO3 (20 eq.) and Pd(PPh3)4 (0.05 eq.) were taken up in 4:1 MeCN/water (0.7 mL) and heated to 160° C. for 15 minutes under microwave irradiation. The mixture was diluted with 1:1 EtOAc/water (6 mL), filtered through GF/F paper, and the layers were separated. The organic layer was dried over MgSO4, filtered, and concentrated to afford 2,6-difluoro-N-(2-(1-methyl-1H-indol-5-yl)-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)-3-(propylsulfonamido)benzamide (19 mg, 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338452B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-33c486bca3eb4334a79d8e5cc7823701 |
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| Source note | uspto-grants-2012_12 |
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